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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068262Generated: October 30, 2026

Diazomethane → HCID 53984498, compound

https://huagongshe.com/reaction/1068262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantHCID 21195227HCID 21195227—
SolventDiethyl EtherHCID 3283—
ProductHCID 53984498HCID 5398449896%

Reaction Steps

A freshly prepared solution of diazomethane in anhydrous ether was added in excess to a solution of N-[2-(2-tert-butylphenylcarboxy)-1,1-dimethylethyl]-trifluoromethanesulfonamide (13.1 g) in ether. The resulting yellow solution was allowed to stand at RT overnight, then was washed with 10% HCl followed by 2.5N aq NaOH. The organic solution was dried (MgSO4), and concentrated to afford 13.0 g of pure N-methyl-N-[2-(2-tert-butylphenylcarboxy)-1,1-dimethylethyl]-trifluoromethanesulfonamide as a white solid, a 96% yield. m.p. 42-44° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248894B1
Source datasetuspto-grants-2001_06
ORD IDord-c68ecd89a9dc407394acbf6a6c4eca84
Source noteuspto-grants-2001_06